anagrelide hydrochloride - Medications
Browse 1 medications containing anagrelide hydrochloride. Open a product record to review formulation details, related brands, manufacturers, and label-backed information.
Anagrelide hydrochloride, USP is a platelet-reducing agent. Its chemical name is 6,7-dichloro-1,5-dihydroimidazo[2,1-b]quinazolin-2(3H)-one monohydrochloride monohydrate. The molecular formula is C 10 H 7 Cl 2 N 3 O•HCl•H 2 O which corresponds to a molecular weight of 310.59. The structural formula is: Anagrelide hydrochloride is an off-white powder. It is very slightly soluble in water and sparingly soluble in dimethyl sulfoxide and dimethylformamide. Each Anagrelide Capsule USP, for oral administration, contains either 0.5 mg or 1 mg of anagrelide base (as anagrelide hydrochloride, USP) and has the following inactive ingredients: anhydrous lactose, microcrystalline cellulose, crospovidone, povidone, sodium lauryl sulfate and magnesium stearate. The hard gelatin capsules contain titanium dioxide, gelatin, FD&C Red No. 40 and purified water. The 0.5 mg capsules also contain black iron oxide, and FD&C Red No. 3. The 1 mg capsules also contain FD&C Blue No. 1, and FD&C Yellow No. 6. In addition, the black imprinting ink contains black iron oxide, butyl alcohol, dehydrated alcohol, isopropyl alcohol, potassium hydroxide, propylene glycol, shellac and ammonia. structure
About anagrelide hydrochloride
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